Ploagents a. HX in. Na2/NH3 b HBr,H2O2, hv n. H2SO2HgSO4 c. H2O,H3SO4 a ( elahal then H2O2. NaOH d. x0 . 1 equinalent of NaNH2 e. H2,Pd a. NES, bv f. x2H2O f. x2, th 9OsO4 then NaHSO3 a. (CH, CH3COK. h. HoiOAche H2O then NaBH4 i. Pery 1. BH3 then H2O2,NiCH1 (4 SOCl2 i. O3 then (CH2L2S v. H2PO4 k. 2 equvaients of NaNis, w H3CrO4 c. PCC y. 10i This synthesis was designed using the Organic Chemistry Rosd Map found in the appendic of your teatbosk. In this syathesis, reagents from the table are vied to carry out the indicated ateps (Wews in blue), in the bor below, draw the structure of compeund a. - Use the weogechash bond tools to indcate stereochemivery where it eaviti. - ir the resction produces a racemic mixture, draw both stereoisemers. - Ir both () and (2) focms of the alkene can be preductd in the resction, draw both isomers. - Separate structures with + shns from the drop-down menu. - In the table of rebenta, x can refer to elther br or a